Hydrohalogenation of N-acetyl(aroyl)-1,4-benzoquinone monoimines

Autor:	Svetlana A. Konovalova, A. P. Avdeenko, O. N. Ludchenko, O. P. Ledeneva, A. V. Vakulenko
Rok vydání:	2011
Předmět:	Chlorophenol 1 4-Benzoquinone chemistry.chemical_compound chemistry Organic Chemistry Ionic bonding Hydrohalogenation Ring (chemistry) Photochemistry Medicinal chemistry
Zdroj:	Russian Journal of Organic Chemistry. 47:214-229
ISSN:	1608-3393 1070-4280
DOI:	10.1134/s1070428011020102
Popis:	New N-acetyl-1,4-benzoquinone monoimines alkyl-substituted in the quinoid ring were synthesized. The hydrohalogenation of N-acetyl(aroyl)-1,4-benzoquinone monoimines proceeds exclusively in keeping with the 1,4-addition. The hydrochlorination occurs along the ionic mechanism, in the hydrobromination grows the role of the radical mechanism.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::607a805cff3aeb9fe1d91896d1977183 https://doi.org/10.1134/s1070428011020102 Zobrazit plný text záznamu Plný text ve formátu PDF